Hurko O - Search Results

1

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

Chomyn A, Martinuzzi A, Yoneda M, Daga A, Hurko O, Johns D, Lai ST, Nonaka I, Angelini C, Attardi G. Chomyn A, et al. Among authors: hurko o. Proc Natl Acad Sci U S A. 1992 May 15;89(10):4221-5. doi: 10.1073/pnas.89.10.4221. Proc Natl Acad Sci U S A. 1992. PMID: 1584755 Free PMC article.

2

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy.

Yoneda M, Chomyn A, Martinuzzi A, Hurko O, Attardi G. Yoneda M, et al. Among authors: hurko o. Proc Natl Acad Sci U S A. 1992 Dec 1;89(23):11164-8. doi: 10.1073/pnas.89.23.11164. Proc Natl Acad Sci U S A. 1992. PMID: 1454794 Free PMC article.

3

Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy.

Hofhaus G, Johns DR, Hurko O, Attardi G, Chomyn A. Hofhaus G, et al. Among authors: hurko o. J Biol Chem. 1996 May 31;271(22):13155-61. doi: 10.1074/jbc.271.22.13155. J Biol Chem. 1996. PMID: 8662757 Free article.

4

The multiple ADP/ATP translocase genes are differentially expressed during human muscle development.

Lunardi J, Hurko O, Engel WK, Attardi G. Lunardi J, et al. Among authors: hurko o. J Biol Chem. 1992 Aug 5;267(22):15267-70. J Biol Chem. 1992. PMID: 1639771 Free article.

5

Mitochondrial leucine tRNA mutation in neurological diseases.

Johns DR, Hurko O. Johns DR, et al. Among authors: hurko o. Lancet. 1991 Apr 13;337(8746):927-8. doi: 10.1016/0140-6736(91)90272-q. Lancet. 1991. PMID: 1673015 Free article. No abstract available.

6

Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.

Johns DR, Rutledge SL, Stine OC, Hurko O. Johns DR, et al. Among authors: hurko o. Proc Natl Acad Sci U S A. 1989 Oct;86(20):8059-62. doi: 10.1073/pnas.86.20.8059. Proc Natl Acad Sci U S A. 1989. PMID: 2813377 Free PMC article.

7

Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNA.

Johns DR, Hurko O. Johns DR, et al. Among authors: hurko o. Genomics. 1989 Oct;5(3):623-8. doi: 10.1016/0888-7543(89)90032-3. Genomics. 1989. PMID: 2533162

8

Identical mitochondrial DNA deletion in blood and muscle.

Johns DR, Drachman DB, Hurko O. Johns DR, et al. Among authors: hurko o. Lancet. 1989 Feb 18;1(8634):393-4. doi: 10.1016/s0140-6736(89)91779-0. Lancet. 1989. PMID: 2563557 Free article. No abstract available.

9

Dystrophin and Duchenne's muscular dystrophy.

Hurko O, Johns DR. Hurko O, et al. N Engl J Med. 1989 Aug 10;321(6):398-9. doi: 10.1056/NEJM198908103210616. N Engl J Med. 1989. PMID: 2664525 No abstract available.

10

Multiple mitochondrial DNA deletions in myo-neuro-gastrointestinal encephalopathy syndrome.

Johns DR, Threlkeld AB, Miller NR, Hurko O. Johns DR, et al. Among authors: hurko o. Am J Ophthalmol. 1993 Jan;115(1):108-9. doi: 10.1016/s0002-9394(14)73533-0. Am J Ophthalmol. 1993. PMID: 8420360 Free article. No abstract available.

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